Issue 38, 2020

Interaction of natural flavonoid eriocitrin with β-cyclodextrin and hydroxypropyl-β-cyclodextrin: an NMR and molecular dynamics investigation

Abstract

It is well known that flavanones have beneficial health effects. Eriodictyol-7-rutinoside, also called eriocitrin, is a flavanone with many positive effects. Like many of these compounds, low water solubility, stability and shelf life are major issues. Many studies have focused on improving these aspects. Towards this goal, β-cyclodextrin and its derivatives are interesting candidates. These compounds are characterized by a hydrophobic central cavity that usually enhances ligand solubility in aqueous solutions, affecting the chemical characteristics of the encapsulated ligand. Recently, eriocitrin/hydroxypropyl-β-cyclodextrin complex with advanced properties has been reported. Herein, computational approaches were combined with NMR spectroscopy to characterize the eriocitrin/β-cyclodextrin complex and compare it with that of eriocitrin/hydroxypropyl-β-cyclodextrin.

Graphical abstract: Interaction of natural flavonoid eriocitrin with β-cyclodextrin and hydroxypropyl-β-cyclodextrin: an NMR and molecular dynamics investigation

Supplementary files

Article information

Article type
Paper
Submitted
22 Apr 2020
Accepted
01 Sep 2020
First published
03 Sep 2020

New J. Chem., 2020,44, 16431-16441

Interaction of natural flavonoid eriocitrin with β-cyclodextrin and hydroxypropyl-β-cyclodextrin: an NMR and molecular dynamics investigation

A. Cesari, G. Uccello Barretta, K. N. Kirschner, M. Pappalardo, L. Basile, S. Guccione, C. Russotto, M. R. Lauro, F. Cavaliere and F. Balzano, New J. Chem., 2020, 44, 16431 DOI: 10.1039/D0NJ02022B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements